Canonical Allele Identifier: CA1926189982

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960944G= , CM000672.2:g.87960944G=	GRCh38
NC_000010.10:g.89720701G= , CM000672.1:g.89720701G=	GRCh37
NC_000010.9:g.89710681G=	NCBI36
NG_007466.2:g.102506G= , LRG_311:g.102506G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.945G=	ENSP00000514759.2:p.Glu315=
ENST00000710265.1:c.852G=	ENSP00000518161.1:p.Glu284=
ENST00000472832.3:c.852G=	ENSP00000483066.2:p.Glu284=
ENST00000688158.2:n.1587G=
ENST00000688922.2:c.*682G=	ENSP00000508742.2:n.*682G=
ENST00000700021.1:c.807G=	ENSP00000514757.1:p.Glu269=
ENST00000700022.1:c.*191G=	ENSP00000514758.1:n.*191G=
ENST00000700023.1:n.2010G=
ENST00000700024.1:n.2244G=
ENST00000700025.1:n.1621G=
ENST00000700026.1:n.489G=
ENST00000700029.1:c.779G=
ENST00000706954.1:c.852G=	ENSP00000516674.1:p.Glu284=
ENST00000706955.1:c.*887G=	ENSP00000516675.1:n.*887G=
ENST00000686459.1:c.*438G=	ENSP00000508909.1:n.*438G=
ENST00000688158.1:c.*963G=	ENSP00000509254.1:n.*963G=
ENST00000688308.1:c.852G=	ENSP00000508752.1:p.Glu284=
ENST00000688922.1:c.773G=
ENST00000693560.1:c.1371G=	ENSP00000509861.1:p.Glu457=
ENST00000371953.8:c.852G= MANE Select	ENSP00000361021.3:p.Glu284=
ENST00000371953.7:c.852G=	ENSP00000361021.3:p.Glu284=
ENST00000472832.2:c.279G=	ENSP00000483066.1:p.Glu93=
NM_000314.5:c.852G=	NP_000305.3:p.Glu284=
NM_000314.6:c.852G=	NP_000305.3:p.Glu284=
NM_001304717.2:c.1371G=	NP_001291646.2:p.Glu457=
NM_001304718.1:c.261G=	NP_001291647.1:p.Glu87=
XM_006717926.2:c.807G=	XP_006717989.1:p.Glu269=
XM_011539981.1:c.852G=	XP_011538283.1:p.Glu284=
XM_011539982.1:c.756G=	XP_011538284.1:p.Glu252=
XR_945791.1:n.1422G=
NM_000314.7:c.852G=	NP_000305.3:p.Glu284=
NM_001304717.5:c.1371G=	NP_001291646.4:p.Glu457=
NM_001304718.2:c.261G=	NP_001291647.1:p.Glu87=
NM_000314.8:c.852G= MANE Select	NP_000305.3:p.Glu284=